Variant report

Variant	rs993352
Chromosome Location	chr10:23307206-23307207
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 17 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:17)

rs_ID	r²[population]
rs10741013	0.84[JPT][hapmap];0.95[MEX][hapmap];0.82[TSI][hapmap]
rs10741014	0.83[CHB][hapmap];0.89[JPT][hapmap];0.84[ASN][1000 genomes]
rs10764372	0.83[CHB][hapmap];0.88[CHD][hapmap];0.86[GIH][hapmap];1.00[JPT][hapmap];0.95[MEX][hapmap];0.89[TSI][hapmap];0.89[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs10828393	0.83[CHD][hapmap];0.86[MEX][hapmap]
rs10828401	0.82[AMR][1000 genomes]
rs1148302	0.84[JPT][hapmap]
rs1382580	0.84[AMR][1000 genomes]
rs4747451	0.90[JPT][hapmap]
rs4748832	0.87[MEX][hapmap]
rs4748835	0.87[CHD][hapmap];0.85[JPT][hapmap]
rs7070539	0.83[CHB][hapmap];0.88[CHD][hapmap];0.95[JPT][hapmap];0.84[ASN][1000 genomes]
rs7075999	0.88[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs7079729	0.88[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs7080677	0.83[CHB][hapmap];1.00[JPT][hapmap];0.87[ASN][1000 genomes]
rs7898352	0.85[GIH][hapmap];0.86[MEX][hapmap]
rs7914172	0.83[CHB][hapmap];0.88[CHD][hapmap];0.95[JPT][hapmap]
rs7917324	0.83[CHB][hapmap];0.95[JPT][hapmap]

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs993352	C10orf67	cis	parietal	SCAN

Chromatin state (count:1 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:23301400-23311200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin

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Input of quick search could be:

dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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